RENAL RESISTIVE INDEX POST-OPERATIVE COMPLICATIONS IN MAJOR SURGERY?

Outcome Clinical Trial

Official title:

MAY RENAL RESISTIVE INDEX BE AN EARLY PREDICTIVE TOOL OF POST-OPERATIVE COMPLICATIONS IN MAJOR SURGERY?

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02041403
• Other study ID #: CE ICH-158/12
• Status: Completed
• Phase: N/A
• First received: January 18, 2014
• Last updated: January 21, 2014
• Start date: June 2012
• Est. completion date: July 2013

Study information

• Verified date: January 2014
• Source: Istituto Clinico Humanitas
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: Ethics Committee
• Study type: Observational

Clinical Trial Summary

An observational trial aiming to verify whether does any relationship exist between renal resistive index and postoperative outcome in major high risk surgery

Description:

Renal resistive index was measured just after major high risk operations and then patients were observed searching for any surgical and medical-related complications during the first post-operative week

Recruitment information / eligibility

• Status: Completed
• Enrollment: 218
• Est. completion date: July 2013
• Est. primary completion date: June 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• age > 18 years

• major surgical operations

Exclusion Criteria:

• age < 18 years

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Major High Risk Operations
• Outcome
• Postoperative Complications
• Renal Resistive Index

Locations

Country	Name	City	State
Italy	Sant'Ambrogio Clinical Institute - Cardiac Anesthesia Unit	Milano
Italy	Humanitas Research Hospital - Dept. Anesthesia and Intensive Care Unit	Rozzano	Milano

Sponsors (1)

Lead Sponsor	Collaborator
Istituto Clinico Humanitas

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Complications	Recording any postoperative complication occurred within the first postoperative week	7 post-operative days	Yes